EP0619361A2 - Phosphorothionates als Koksbildung-Inhibitoren - Google Patents

Phosphorothionates als Koksbildung-Inhibitoren Download PDF

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Publication number
EP0619361A2
EP0619361A2 EP94302429A EP94302429A EP0619361A2 EP 0619361 A2 EP0619361 A2 EP 0619361A2 EP 94302429 A EP94302429 A EP 94302429A EP 94302429 A EP94302429 A EP 94302429A EP 0619361 A2 EP0619361 A2 EP 0619361A2
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EP
European Patent Office
Prior art keywords
phosphorotrithioate
phosphorothioate
petroleum feedstock
feedstock
heat transfer
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Application number
EP94302429A
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English (en)
French (fr)
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EP0619361B1 (de
EP0619361A3 (de
Inventor
Youndong Tong
Michael K. Poindexter
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Nalco Energy Services LP
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Nalco Chemical Co
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    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G9/00—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
    • C10G9/14—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils in pipes or coils with or without auxiliary means, e.g. digesters, soaking drums, expansion means
    • C10G9/16—Preventing or removing incrustation
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S585/00—Chemistry of hydrocarbon compounds
    • Y10S585/949—Miscellaneous considerations
    • Y10S585/95—Prevention or removal of corrosion or solid deposits

Definitions

  • the invention relates to an antifouling process for treating heat transfer surfaces which heat or cool various hydrocarbon feedstocks, often in the presence of steam, at conditions tending to promote the formation of coke on the surfaces, and more particularly, to; the use of phosphorothioates as anti-coking agents.
  • Ethylene manufacture entails the use of pyrolysis or cracking furnaces to manufacture ethylene from various gaseous and liquid petroleum feedstocks.
  • Typical gaseous feedstocks include ethane, propane, butane and mixtures thereof.
  • Typical liquid feedstocks include naphthas, kerosene, and atmospheric/vacuum gas oil.
  • gaseous or liquid hydrocarbon feedstocks are pyrolyzed in the presence of steam, significant quantities of ethylene and other useful unsaturated compounds are obtained.
  • Steam is used to regulate the cracking reaction of saturated feedstocks to unsaturated products. The effluent products are quenched and fractionated in downstream columns, and then further reacted or processed depending on need.
  • Fouling of cracking furnace coils, transfer line exchangers (TLEs) and other heat transfer surfaces occurs because of coking and polymer deposition.
  • the fouling problem is one of the major operational limitations experienced in running an ethylene plant. Depending on deposition rate, ethylene furnaces must be periodically shut down for cleaning. In addition to periodic cleaning, crash shutdowns are sometimes required because of dangerous increases in pressure or temperatures resulting from deposit buildup in the furnace coils and TLEs. Cleaning operations are carried out either mechanically or by passing steam and/or air through the coils to oxidize and burn off the coke buildup.
  • a major limitation of ethylene furnace run length is coke formation in the radiant section and transfer line exchangers (TLEs).
  • the coke is normally removed by introducing steam and/or air to the unit which in effect burns off carbonaceous deposits. Since coke is a good thermal insulator, the furnace firing must be gradually increased to provide enough heat transfer to maintain the desired conversion level. Higher temperatures shorten the tube life, and tubes are quite expensive to replace. Additionally, coke formation decreases the effective cross-sectional area of the process gas, which increases the pressure drop across the furnace and TLEs. Not only is valuable production time lost during the decoking operation, but also the pressure buildup resulting from coke formation adversely affects ethylene yield.
  • Run lengths for ethylene furnaces average from one week to four months depending in part upon the rate of fouling of the furnace coils and TLEs. This fouling rate is in turn dependent upon the nature of the feedstock as well as upon furnace design and operational parameters. In general, however, heavier feedstocks and higher cracking severity results in an increased rate of furnace and TLE fouling. A process or additive that could increase run length would lead to fewer days lost to decoking and lower maintenance costs.
  • Convection section corrosion has been a problem with many phosphorus-based anticoking additives of the prior art.
  • conditions are constantly changing. Heated steam and hydrocarbon are typically introduced to the section separately and then mixed well before entering the radiant section.
  • Heated steam and hydrocarbon are typically introduced to the section separately and then mixed well before entering the radiant section.
  • a product which is an excellent coke suppressant may also be an extremely corrosive species if it accumulates in the convection section.
  • additives Once additives pass through the convection, radiant, and TLE sections, they are subject to effluent quench conditions.
  • heavy products concentrate in the primary fractionator, water quench tower, caustic tower and/or compressor knock-out drums, while the lighter components are collected in columns downstream of the compressors.
  • Accumulation of coke inhibitors and their cracked by-products is dictated mainly by their physical properties. Briefly, inhibitor by-products with high boiling points are condensed early in the fractionation process while lighter ones progress to the later stages.
  • phosphorus-containing products are good ligands and can adversely affect the catalyst performance.
  • the phosphorus by-product which is of greatest concern is phosphine (PH3).
  • This by-product is extremely low-boiling (-88°C). In fact, it has basically the same boiling point as acetylene (-84°C), a hydrocarbon by-product which is often catalytically hydrogenated to the more desired ethylene.
  • the present invention is a method for the use of a new antifoulant and coke suppressant, trisubstituted phosphorothioate, to reduce fouling in various high temperature applications, including steam cracking furnaces.
  • the phosphorothioate is used to treat heat transfer surfaces used to heat or cool a petroleum feedstock at coke-forming conditions.
  • the heat transfer surfaces can be contacted with the inhibitor in several different ways, including, for example, pretreating the heat transfer surfaces prior to heating or cooling the petroleum feedstock, continuously or intermittently adding a trace amount of the additive to the petroleum feedstock as it is being heated or cooled, adding the phosphorothioate to steam feed which is then mixed with the petroleum feedstock, to the petroleum feedstock itself, or to a feed mixture of the petroleum feedstock and steam, and the like.
  • the additive is preferably added at a rate from about 0.1 to about 1000 ppm, on a basis of elemental phosphorus in the phosphorothioate additive, more preferably from about 1 to about 100 ppm, by weight of the petroleum feedstock.
  • Each R in the foregoing phosphorothioate formula is preferably alkyl, aryl, alkylaryl, or arylalkyl, wherein the phosphorothioate preferably has from 3 to about 45 carbon atoms, and more preferably, each R has from 1 to 15 carbon atoms.
  • coke formation is defined as any buildup of coke or coke precursors on the heat transfer surfaces, including convection coils, radiant furnace coils, transfer line exchangers, quench towers, or the like.
  • Other phosphorus-containing compounds have been disclosed in various patents and other references as effective coke formation inhibitors. However, none of the phosphorus compounds provide the same performance as the present phosphorothioates. Performance is based not only on the anticoking agent's ability to suppress and inhibit coke formation, but just as importantly, on being essentially free from causing any harmful side effects associated with many of the prior art additives, such as contributing to corrosion or impairing catalyst performance.
  • petroleum feedstock is used to refer to any hydrocarbon generally heated or cooled at the heat transfer surfaces, regardless of the degree of previous processing, and specifically when used in reference to an ethylene or other cracking furnace, refers to the hydrocarbon before processing, as well as the hydrocarbon during and after processing in the furnace itself, in the TLE, in the quench section, etc.
  • the feedstock can include ethane, butane, kerosene, naphtha, gas oil, combinations thereof, and the like.
  • Fig. 1 is a graph illustrating the relative corrosion rates of various phosphorus compounds.
  • the coking inhibitor of the present invention is a phosphorus and sulfur-based compound which is essentially non-corrosive and is essentially free from phosphine formation under general coking conditions.
  • the present anti-coking agent has the following general formula: wherein X is chalcogen, preferably oxygen, and especially sulfur; wherein Y is chalcogen, preferably sulfur, and especially oxygen, provided that when X is oxygen, Y is sulfur; and wherein each R is independently hydrocarbyl, such as, for example, alkyl, aryl, alkylaryl, arylalkyl, or the like, and two or more of R taken together can form a heterocyclic moiety.
  • the anti-coking agent is referred to herein generally as the preferred S,S,S-trihydrocarbyl phosphorotrithioate, or simply as phosphorotrithioate.
  • the phosphorotrithioate preferably has from 3 to about 45 carbon atoms and each R group preferably comprises from 1 to 15 carbon atoms. If the number of carbon atoms in the phosphorotrithioate is excessively large, the economics of the additive are less favorable, the additive can lose volatility and miscibility to mix properly in the petroleum feedstock being treated, or can lose the desired stability.
  • the hydrocarbyl groups can be substituted with or contain a heteroatom such as a chalcogen, pnicogen, or the like, but this is generally less preferred because of the concomitant instability imparted by the heteroatom.
  • the heteroatom will impart solubility in steam or water
  • the presence of a heteroatom can be useful, especially where the heteroatom is in a terminal portion of the hydrocarbyl group spaced from the phosphorotrithioate moiety, so that any cleavage or other reaction of the heteroatom will leave the phosphorotrithioate moiety substantially intact for anticoking effectiveness.
  • the hydrocarbyl group can be the same or different in each thiol moiety, for example, where the phosphorotrithioate is formed from a mixture of different thiols, and/or reacted with different thiols in a stepwise fashion. In of different thiols, and/or reacted with different thiols in a stepwise fashion. In many instances, it is not necessary that the phosphorotrithioate be completely pure, and the reaction product obtained by using isomers or mixtures of thiols, which may be more economically available than the pure thiols, are generally suitable.
  • anticoking additives include S,S,S-tributyl phosphorotrithioate; S,S,S-triphenyl phosphorotrithioate; and the like.
  • the phosphorotrithioates are prepared according to methods known in the art, and in some cases are already commercially available. Generally, the phosphorotrithioates can be prepared by the reaction of phosphorus oxyhalide, e.g. phosphorus oxybromide or phosphorus oxychloride, with an excess of thiol in a suitable solvent such as heavy aromatic naphtha, toluene, benzene, etc., with evolution of the corresponding hydrohalide. Bases may also be incorporated to help drive the desired transformation.
  • phosphorus oxyhalide e.g. phosphorus oxybromide or phosphorus oxychloride
  • the phosphorotrithioate is used to inhibit coke formation on heat transfer surfaces used most often to heat, but sometimes to cool, petroleum feedstocks at coke-forming conditions, by treating the surfaces with an effective amount of the phosphorotrithioate.
  • the surface can be effectively treated, for example, by introducing the phosphorotrithioate into the petroleum feedstock before the feedstock comes into contact with the heat transfer surfaces.
  • the phosphorotrithioate can be used in an amount effective to obtain the desired inhibition of coke formation, usually at least 0.1 ppm by weight in the hydrocarbon, preferably at least 1 ppm, on a basis of elemental phosphorus. There is usually no added benefit in using the phosphorotrithioate in a relatively high concentration, and the economics are less favorable.
  • the phosphorotrithioate is used in an amount from about 0.1 to about 1000 ppm, more preferably from about 1 to about 100 ppm, by weight in the hydrocarbon, or an elemental phosphorus basis.
  • the addition to the petroleum feedstock is preferably continuous, but it is also possible to use the petroleum feedstock treatment on an intermittent basis, depending on the coke inhibition which is desired in the particular application. For example, where there is a scheduled shutdown of the heat transfer equipment for maintenance, other than for the build up of coke deposits, the continuous addition of the phosphorotrithioate to the petroleum feedstock could be terminated in advance of the shutdown. Or, the anti-coking agent could be used in the petroleum feedstock after the development of a pressure drop through the heat transfer equipment indicative of coke formation therein.
  • the heat transfer surfaces before they come into contact with the petroleum feedstock, for example, by applying the phosphorotrithioate as a pretreatment or as a treatment between production runs.
  • the phosphorotrithioate can be circulated through the heat transfer equipment, preferably in a suitable diluent.
  • the heat transfer equipment can also be filled with the phosphorotrithioate solution and allowed to soak for a period of time to form a protective film on the heat transfer surfaces.
  • the petroleum feedstock can be dosed at a relatively high initial rate, for example, at the beginning of a run, e.g. 0.5 to 2.0 weight percent, and after a period of time, e.g. 1 to 24 hours, reduced to the continuous dosage rates described above.
  • the phosphorotrithioate is preferably added as a solution in a master batch.
  • the mode of blending the phosphorotrithioate with the feedstock is not particularly critical, and a vessel with an agitator is all that is required.
  • a master batch of the phosphorotrithioate in a suitable solvent, such as aliphatic or aromatic hydrocarbon is metered into a stream of the feedstock and intimately mixed therein by turbulence in the processing equipment.
  • the phosphorotrithioate can be added to a steam or water stream which is injected or otherwise added to the petroleum feedstock stream, or the phosphorotrithioate can be added to a mixed stream of the petroleum feedstock and steam or water.
  • the phosphorotrithioate should be added to the feedstock upstream of the heat transfer surfaces being treated.
  • the phosphorotrithioate addition should be sufficiently upstream to allow sufficient mixing and dispersion of the additive in the feedstock, but preferably not so far upstream so as to avoid or minimize any significant decomposition or degradation of the phosphorotrithioate.
  • a laboratory reactor was used to duplicate conditions in an ethylene furnace as closely as possible. Coke formation was measured on a coupon constructed of 321 stainless steel placed in the lab reactor. To maintain constant cracking conditions, the ethylene to propylene ratio was kept at 2.0. The reaction temperature was about 700°C throughout each run. Argon was used as a dilution media (5 l/hr). The additive being evaluated was mixed with the hydrocarbon prior to cracking so that the reactor feed had a constant additive content. The coupon was suspended in a vertical run of the furnace from a balance equipped with a digital display and a digital-analog converter to record coking rates. The temperature profile of the reactor was measured off-line using a thermal element inserted inside the reactor tube under identical flow conditions as during the experiment.
  • the recorded reaction temperatures were measured in the isothermal section of the reactor, where the coupon is located. Temperatures at the outer wall of the reactor tube which were continuously monitored during the experiment were approximately 20°C higher than the recorded reaction temperature.
  • Each coupon was ultrasonically cleaned with acetone. A new coupon was used for each new experiment. After each new coupon was inserted into the reactor tube, the scale was calibrated, the reactor was evacuated several times and flushed with argon to remove traces of air. Coupons were activated by alternate exposure in the reactor tube to cracking conditions with n-heptane for ten minutes and decoking conditions with air until the coke was completely removed.
  • a high temperature wheel box was used to determine the degradative properties of various additives over long periods of time.
  • Additive A was used at a concentration of 5 percent in n-heptane, and other additives were used at an equivalent phosphorus content.
  • the additive was added to a high alloy vessel along with hydrocarbon, varying amounts of water and preweighed coupons constructed of carbon steel. The contents were rotated continuously at temperatures representative of a typical convection section of an ethylene furnace; the mixing ensured that the coupons would be exposed to both a liquid and a gas phase (composed of water and hydrocarbon). Exposing the additives to high temperature for extended periods of time permitted potential decomposition to harmful by-products.
  • this method simulated a worse case scenario involving a fairly high concentration of an additive in the convection section with eventual accumulation/degradation (e.g. thermolysis, hydrolysis, disproportionation, etc.) to by-products which may or may not be corrosive. Additionally, the appearance of corrosion may not be the direct result of degradation, but may be an inherent property of an additive.
  • test data for Additive A is compared against two other compounds, one of which was an amine-neutralized phosphate ester mono- and di-substituted with alkyl groups, a known coke suppressant with aggressive corrosivity.
  • the S,S,S,-tributyl phosphorotrithioate (A) exhibited excellent performance no matter how much water was present. The same was not true for the other phosphorus-based compounds.
  • a lab unit was constructed which would simulate the dynamic (i.e. erosive and corrosive) conditions of a typical convection section of an ethylene furnace. Corrosion is more likely to occur at or near the bends/elbows of the convection sections because of high erosion due to the velocity of the stream.
  • Steam, generated from one vessel was mixed with hydrocarbon (hexane and toluene at 50-50 weight percent) from a second vessel (steam:hydrocarbon weight ratio 0.5-0.6). Heating to the desired temperature was accomplished by passing the mixture through two independent furnaces held at specified temperatures (100-600°C). Both furnaces were monitored and controlled via two separate temperature controllers. Preweighed corrosion coupons, made of carbon steel, were situated at a bend within the furnace coil.
  • Coupon A was situated in the process flow, subjected to the erosive and corrosive nature of the process stream.
  • Coupon B was situated in a dead-leg projecting out of the bend of interest. This positioning permitted the accumulation of corrosive species, but shielded Coupon B from the nearby erosive environment. In essence, Coupon B was situated to study the effects of points where the process flow is extremely dormant (i.e. non-turbulent areas). Thermocouples were used to record the temperature of both coupons as well as both furnace sections.
  • additives were evaluated in the apparatus described in the Example 4. Additive A was used at 5 weight percent in the hydrocarbon, and all other additives were used at an equivalent phosphorus content. To achieve the proper cracking temperature, a radiant section (750-950°C) was added just after the convection section. To more accurately simulate a typical ethylene furnace downstream quenching process, the effluent gases were passed through several vessels maintained at a low temperature (0°C and -78°C), a caustic scrubber, and a dryer containing 3 ⁇ molecular sieves.
  • the cracked gas effluent was bubbled through deuterated chloroform at low temperatures (-78°C) and analyzed by 31PNMR at -60°C. The spectrum obtained matched PH3 from the literature (-234 ppm, quartet with J PH 192 Hz). TABLE 5 ADDITIVE RELATIVE PH3 FORMATION RATE A 0.7 B 0.4 C 0.4 F 100 G >250

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  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
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  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Thermal Sciences (AREA)
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EP94302429A 1993-04-07 1994-04-06 Phosphorothionates als Koksbildung-Inhibitoren Expired - Lifetime EP0619361B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US44183 1993-04-07
US08/044,183 US5354450A (en) 1993-04-07 1993-04-07 Phosphorothioate coking inhibitors

Publications (3)

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EP0619361A2 true EP0619361A2 (de) 1994-10-12
EP0619361A3 EP0619361A3 (de) 1995-01-11
EP0619361B1 EP0619361B1 (de) 1998-08-05

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EP94302429A Expired - Lifetime EP0619361B1 (de) 1993-04-07 1994-04-06 Phosphorothionates als Koksbildung-Inhibitoren

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US (1) US5354450A (de)
EP (1) EP0619361B1 (de)
JP (1) JP2944882B2 (de)
AT (1) ATE169328T1 (de)
AU (1) AU660867B2 (de)
BR (1) BR9304384A (de)
DE (1) DE69412161T2 (de)
ES (1) ES2122164T3 (de)
TW (1) TW263528B (de)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0837119A2 (de) * 1996-10-18 1998-04-22 Nalco/Exxon Energy Chemicals, L.P. Verfahren zur Abgabe von Mittel zur Verhinderung von Ablagerungen in Heizgeräte
EP1085074A2 (de) * 1999-09-15 2001-03-21 Nalco/Exxon Energy Chemicals L.P. Mittel zur Verhinderung von Ablagerungen auf Basis von Fosfor und Schwefel
WO2004007642A1 (en) * 2002-07-16 2004-01-22 Dorf Ketal Chemicals India Pvt. Ltd. Method for reducing foam in a primary fractionator
US7575669B2 (en) 2002-06-26 2009-08-18 Dorf Ketal Chemicals, Llc Method of removal of carbonyl compounds along with acid gases from cracked gas in ethylene process

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5779881A (en) * 1994-02-03 1998-07-14 Nalco/Exxon Energy Chemicals, L.P. Phosphonate/thiophosphonate coking inhibitors
US5500107A (en) * 1994-03-15 1996-03-19 Betz Laboratories, Inc. High temperature corrosion inhibitor
US5552085A (en) * 1994-08-31 1996-09-03 Nalco Chemical Company Phosphorus thioacid ester inhibitor for naphthenic acid corrosion
US5954943A (en) * 1997-09-17 1999-09-21 Nalco/Exxon Energy Chemicals, L.P. Method of inhibiting coke deposition in pyrolysis furnaces
US6482311B1 (en) 2000-08-01 2002-11-19 Tda Research, Inc. Methods for suppression of filamentous coke formation
US6454995B1 (en) 2000-08-14 2002-09-24 Ondeo Nalco Energy Services, L.P. Phosphine coke inhibitors for EDC-VCM furnaces
US6368494B1 (en) 2000-08-14 2002-04-09 Nalco/Exxon Energy Chemicals, L.P. Method for reducing coke in EDC-VCM furnaces with a phosphite inhibitor
US7056399B2 (en) * 2003-04-29 2006-06-06 Nova Chemicals (International) S.A. Passivation of steel surface to reduce coke formation
US8466096B2 (en) * 2007-04-26 2013-06-18 Afton Chemical Corporation 1,3,2-dioxaphosphorinane, 2-sulfide derivatives for use as anti-wear additives in lubricant compositions
US20110100015A1 (en) * 2009-11-05 2011-05-05 General Electric Company Gas turbine system to inhibit coke formation and methods of use

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US4024049A (en) * 1975-01-07 1977-05-17 Nalco Chemical Company Mono and di organophosphite esters as crude oil antifoulants
US4542253A (en) * 1983-08-11 1985-09-17 Nalco Chemical Company Use of phosphate and thiophosphate esters neutralized with water soluble amines as ethylene furnace anti-coking antifoulants

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US3531394A (en) * 1968-04-25 1970-09-29 Exxon Research Engineering Co Antifoulant additive for steam-cracking process
US4024050A (en) * 1975-01-07 1977-05-17 Nalco Chemical Company Phosphorous ester antifoulants in crude oil refining
US4024051A (en) * 1975-01-07 1977-05-17 Nalco Chemical Company Using an antifoulant in a crude oil heating process
US4024048A (en) * 1975-01-07 1977-05-17 Nalco Chemical Company Organophosphorous antifoulants in hydrodesulfurization
US4105540A (en) * 1977-12-15 1978-08-08 Nalco Chemical Company Phosphorus containing compounds as antifoulants in ethylene cracking furnaces
US4728629A (en) * 1980-08-05 1988-03-01 Phillips Petroleum Company Cracking catalyst restoration with aluminum compounds
US4842716A (en) * 1987-08-13 1989-06-27 Nalco Chemical Company Ethylene furnace antifoulants
US4835332A (en) * 1988-08-31 1989-05-30 Nalco Chemical Company Use of triphenylphosphine as an ethylene furnace antifoulant
US4900426A (en) * 1989-04-03 1990-02-13 Nalco Chemical Company Triphenylphosphine oxide as an ethylene furnace antifoulant
US4941994A (en) * 1989-07-18 1990-07-17 Petrolite Corporation Corrosion inhibitors for use in hot hydrocarbons

Patent Citations (2)

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Publication number Priority date Publication date Assignee Title
US4024049A (en) * 1975-01-07 1977-05-17 Nalco Chemical Company Mono and di organophosphite esters as crude oil antifoulants
US4542253A (en) * 1983-08-11 1985-09-17 Nalco Chemical Company Use of phosphate and thiophosphate esters neutralized with water soluble amines as ethylene furnace anti-coking antifoulants

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0837119A2 (de) * 1996-10-18 1998-04-22 Nalco/Exxon Energy Chemicals, L.P. Verfahren zur Abgabe von Mittel zur Verhinderung von Ablagerungen in Heizgeräte
EP0837119A3 (de) * 1996-10-18 1999-01-20 Nalco/Exxon Energy Chemicals, L.P. Verfahren zur Abgabe von Mittel zur Verhinderung von Ablagerungen in Heizgeräte
EP1085074A2 (de) * 1999-09-15 2001-03-21 Nalco/Exxon Energy Chemicals L.P. Mittel zur Verhinderung von Ablagerungen auf Basis von Fosfor und Schwefel
EP1085074A3 (de) * 1999-09-15 2001-11-07 Ondeo Nalco Energy Services, L.P. Mittel zur Verhinderung von Ablagerungen auf Basis von Fosfor und Schwefel
US7575669B2 (en) 2002-06-26 2009-08-18 Dorf Ketal Chemicals, Llc Method of removal of carbonyl compounds along with acid gases from cracked gas in ethylene process
WO2004007642A1 (en) * 2002-07-16 2004-01-22 Dorf Ketal Chemicals India Pvt. Ltd. Method for reducing foam in a primary fractionator
US7906012B2 (en) 2002-07-16 2011-03-15 Dorf Ketal Chemicals India Pvt. Ltd. Method for reducing foam in a primary fractionator

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Publication number Publication date
EP0619361B1 (de) 1998-08-05
DE69412161D1 (de) 1998-09-10
BR9304384A (pt) 1994-11-08
AU5496294A (en) 1994-10-13
US5354450A (en) 1994-10-11
TW263528B (de) 1995-11-21
JPH06306369A (ja) 1994-11-01
JP2944882B2 (ja) 1999-09-06
ATE169328T1 (de) 1998-08-15
DE69412161T2 (de) 1999-02-04
EP0619361A3 (de) 1995-01-11
ES2122164T3 (es) 1998-12-16
AU660867B2 (en) 1995-07-06

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